Drug repurposing in skeletal muscle ion channelopathies

Author:

Altamura Concetta,Saltarella Ilaria,Campanale Carmen,Laghetti Paola,Desaphy Jean-FrançoisORCID

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology

Reference56 articles.

1. Ion Channel gene mutations causing skeletal muscle disorders: pathomechanisms and opportunities for therapy;Maggi;Cells,2021

2. Prevalence study of genetically defined skeletal muscle channelopathies in England;Horga;Neurology,2013

3. Prevalence and mutation spectrum of skeletal muscle channelopathies in The Netherlands;Stunnenberg;Neuromuscul Disord,2018

4. Guidelines on clinical presentation and management of nondystrophic myotonias;Stunnenberg;Muscle Nerve,2020

5. Understanding the impact of non-dystrophic myotonia on patients and caregivers: results from a burden of disease healthcare survey;Diaz-Manera;Eur Med (Edicion Espanola) J,2021

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